Unfolding Story of Inclusion-Body Myositis and Myopathies: Role of Misfolded Proteins, Amyloid-β, Cholesterol, and Aging (Q44388796)

2 December 2017

title

Unfolding story of inclusion-body myositis and myopathies: role of misfolded proteins, amyloid-beta, cholesterol, and aging (English)

1 reference

2 December 2017

Unfolding Story of Inclusion-Body Myositis and Myopathies: Role of Misfolded Proteins, Amyloid-β, Cholesterol, and Aging (English)

1 reference

https://api.crossref.org/works/10.1177/08830738030180030401

30 December 2023

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12731644

30 December 2023

author name string

Valerie Askanas

1

1 reference

2 December 2017

W. King Engel

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12731644

30 December 2023

language of work or name

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1 March 2003

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full work available at URL

2 December 2017

http://journals.sagepub.com/doi/pdf/10.1177/08830738030180030401

1 reference

https://api.crossref.org/works/10.1177/08830738030180030401

Journal of Child Neurology

30 December 2023

published in

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2 December 2017

volume

18

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2 December 2017

issue

3

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2 December 2017

page(s)

185-190

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Inflammatory muscle diseases

2 December 2017

cites work

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Inclusion-body myositis: newest concepts of pathogenesis and relation to aging and Alzheimer disease

21 January 2018

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Amyloid-beta deposition in skeletal muscle of transgenic mice: possible model of inclusion body myopathy

21 January 2018

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Inclusion body myositis-like phenotype induced by transgenic overexpression of beta APP in skeletal muscle

21 January 2018

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Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patients.

21 January 2018

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Facioscapulohumeral muscular dystrophy

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The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

21 January 2018

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Distal myopathy with rimmed vacuoles: novel mutations in the GNE gene

21 January 2018

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A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees

21 January 2018

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CSF evaluation in primary CNS lymphoma patients by PCR of the CDR III IgH genes.

21 January 2018

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A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Molecular cloning and functional expression of UDP-N-acetyl-glucosamine 2-epimerase/N-acetylmannosamine kinase

21 January 2018

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Primary structure and expression analysis of human UDP-N-acetyl-glucosamine-2-epimerase/N-acetylmannosamine kinase, the bifunctional enzyme in neuraminic acid biosynthesis

21 January 2018

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UDP-GlcNAc 2-epimerase: a regulator of cell surface sialylation

21 January 2018

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Enhanced detection of congo-red-positive amyloid deposits in muscle fibers of inclusion body myositis and brain of Alzheimer's disease using fluorescence technique

21 January 2018

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Use of anti-neurofilament antibody to identify paired-helical filaments in inclusion-body myositis.

21 January 2018

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Immunocytochemical localization of ubiquitin in inclusion body myositis allows its light‐microscopic distinction from polymyositis

21 January 2018

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Apolipoprotein E and apolipoprotein E messenger RNA in muscle of inclusion body myositis and myopathies

21 January 2018

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The Alzheimer family of diseases: many etiologies, one pathogenesis?

21 January 2018

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Medicine: danger--misfolding proteins.

21 January 2018

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Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases

21 January 2018

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Cellular defenses against unfolded proteins: a cell biologist thinks about neurodegenerative diseases

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Specificity in intracellular protein aggregation and inclusion body formation

21 January 2018

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The unfolding tale of the unfolded protein response

21 January 2018

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Transfer of beta-amyloid precursor protein gene using adenovirus vector causes mitochondrial abnormalities in cultured normal human muscle

21 January 2018

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Beta APP gene transfer into cultured human muscle induces inclusion-body myositis aspects

21 January 2018

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Impaired innervation of cultured human muscle overexpressing betaAPP experimentally and genetically: relevance to inclusion-body myopathies

21 January 2018

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Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle

21 January 2018

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Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositis

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New advances in inclusion-body myositis

30 December 2023

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RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS

30 December 2023

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Ubiquitin immunostaining and inclusion body myositis: study of 30 patients with inclusion body myositis

30 December 2023

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Hereditary inclusion body myopathies

30 December 2023

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30 December 2023

Identifiers

1 reference

Fatcat

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30 July 2022

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Fatcat ID

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Fatcat

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mapped directly with Wikidata item

30 July 2022

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https://api.fatcat.wiki/v0/release/lrikmte5jvc2rpct3t2h2e7dvu

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